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C62794

Sigma-Aldrich

2-Chlorophenol

98%

Synonym(s):

o-Chlorophenol

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About This Item

Linear Formula:
ClC6H4OH
CAS Number:
95-57-8
Molecular Weight:
128.56
Beilstein/REAXYS Number:
1905114
EC Number:
202-433-2
MDL number:
MFCD00002159
UNSPSC Code:
12352100
PubChem Substance ID:
24892853
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.558 (lit.)

bp

175-176 °C (lit.)

mp

8 °C (lit.)

density

1.241 g/mL at 25 °C (lit.)

SMILES string

Oc1ccccc1Cl

InChI

1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H

InChI key

ISPYQTSUDJAMAB-UHFFFAOYSA-N

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Application

2-Chlorophenol is used to synthesize various organic intermediates and compounds including several polycyclic aromatic hydrocarbons and pharmacologically active molecules. It is used as a precursor to synthesize polychlorinated dibenzo p-dioxins and dibenzofurans (PCDD/Fs).

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

flash_point_f

147.2 °F - closed cup

flash_point_c

64.0 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
STBL2070
STBL0092
STBK8530
STBK4742
STBJ3909

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Hydroxyterphenylphoshine- Palladium Catalyst for Benzo [b] furan Synthesis from 2-Chlorophenols. Bifunctional Ligand Strategy for Cross-Coupling of Chloroarenes.
Wang, Jia-Rui and Manabe, Kei
The Journal of Organic Chemistry, 75(15), 5340-5342 (2010)
Synthesis and anti-inflammatory activity evaluation of some novel 6-alkoxy (phenoxy)-[1, 2, 4] triazolo [3, 4-a] phthalazine-3-amine derivatives.
Sun, Xian-Yu et al.
European Journal of Medicinal Chemistry, 45(11), 4807-4812 (2010)
A quantum mechanical study on the formation of PCDD/Fs from 2-chlorophenol as precursor.
Zhang, Qingzhu et al.
Environmental Science & Technology, 42(19), 7301-7308 (2008)
Microwave-promoted Suzuki-Miyaura coupling of arylboronic acids with 1-bromo-2-naphthol, o-bromophenol, and o-chlorophenol.
Wawrzyniak P and Heinicke J.
Tetrahedron Letters, 47(50), 8921-8924 (2006)
Thi Thu Nga Nguyen et al.
The Journal of antimicrobial chemotherapy, 70(3), 731-738 (2014-10-23)
HIV resistance to the integrase inhibitor raltegravir in treated patients is characterized by distinct resistance pathways. We hypothesize that differences in the in vivo dynamics of HIV resistance to raltegravir are due to the genetic context of the integrase present
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